tailieunhanh - Group-based variant calling leveraging next-generation supercomputing for large-scale whole-genome sequencing studies

Next-generation sequencing (NGS) technologies have become much more efficient, allowing whole human genomes to be sequenced faster and cheaper than ever before. However, processing the raw sequence reads associated with NGS technologies requires care and sophistication in order to draw compelling inferences about phenotypic consequences of variation in human genomes. |

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